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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241636Generated: October 31, 2026

Hydrochloric Acid → tert-Butyl 3-sulfanylazetidine-1-carboxylate

https://huagongshe.com/reaction/241636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 3-(acetylthio)azetidine-1-carboxylateHCID 18363257—
SolventMethanolHCID 887—
Producttert-Butyl 3-sulfanylazetidine-1-carboxylateHCID 58513580101.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

Mixture of tert-butyl 3-(acetylthio)azetidine-1-carboxylate (STEP C, 700 mg, 3.03 mmol), methanol (10 mL) and potassium carbonate (836 mg, 6.05 mol) was stirred at 50° C. for 2 h and cooled to room temperature. To the reaction mixture was added 2 mol/L hydrochloric acid for solution acidified (pH <4). The resulting solution was extracted with diethyl ether (30 mL×2). The organic layer was combined and washed with water (30 mL×2) and brine (30 mL). The extract was dried with magnesium sulfate and concentrated. Resulting crude product (581 mg) was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653063B2
Source datasetuspto-grants-2014_02
ORD IDord-1976d53515af40f5b89eae1279a0532d
Source noteuspto-grants-2014_02